ClinVar Miner

List of variants in gene ATP6V0A2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_012463.3(ATP6V0A2):c.-227A>G rs561163813
NM_012463.4(ATP6V0A2):c.*2085C>G rs185883563
NM_012463.4(ATP6V0A2):c.*2128_*2129del rs150303181
NM_012463.4(ATP6V0A2):c.*2485C>T rs144043973
NM_012463.4(ATP6V0A2):c.*785T>C rs146660715
NM_012463.4(ATP6V0A2):c.*998T>C rs12298446
NM_012463.4(ATP6V0A2):c.-117C>T rs532360215
NM_012463.4(ATP6V0A2):c.1258G>T (p.Val420Leu) rs138716143
NM_012463.4(ATP6V0A2):c.1486G>A (p.Ala496Thr) rs143142641
NM_012463.4(ATP6V0A2):c.1698A>G (p.Gly566=) rs2271659
NM_012463.4(ATP6V0A2):c.1724+20del rs375845531
NM_012463.4(ATP6V0A2):c.2294-4G>A rs551697992

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.